Home GUDID 00680243766491
DoublecheQ Pregnancy Test
Primary DI 00680243766491
Brand DoublecheQ Pregnancy Test
Company UNIVERSAL MEDITECH INC.
Model Cassette
Catalog number 100-13
Device description The DoublecheQ Pregnancy Test is designed to be used for a qualitative determination of elevated human chorionic gonadotropin in urine. The result can be read visually in minutes to indicate a positive or negative result for pregnancy.
Published 2019-06-03
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx false
OTC true
Sterile false
Single use true Product Codes# Code, Name table Code Name LCX Kit, Test, Pregnancy, Hcg, Over The Counter
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class LCX Kit, Test, Pregnancy, Hcg, Over The Counter Clinical Chemistry 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00680243766491 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, UPC-A table Source identifier GTIN-14 normalized UPC-A EAN-13 00680243766491 00680243766491 680243766491 0680243766491
GMDN Terms# Term, Definition table Term Definition Total human chorionic gonadotropin (HCG) IVD, kit, immunochromatographic test (ICT), rapid A collection of reagents and other associated materials intended to be used for the qualitative and/or semi-quantitative detection of total human chorionic gonadotropin (HCG), which may include intact HCG, nicked HCG, free alpha-HCG subunits and/or free beta-HCG subunits, in a clinical specimen within a short period, relative to standard laboratory testing procedures, using an immunochromatographic test (ICT) method. This test is commonly used in the laboratory or in point-of-care analyses.
Storage And Handling# Type, Low, High table Type Low High Condition Storage Environment Temperature 36 Degrees Fahrenheit 86 Degrees Fahrenheit
Regulatory Flags# DUNS number 080243910 Device count 1 DM exempt false Premarket exempt false HCT/P false Kit false Combination product false Lot or batch true Serial number false Manufacturing date on label false Expiration date on label true Donation ID number false Contains natural rubber latex false No natural rubber latex false Sterilization required before use false Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published B512100011 One Step Pregnancy Test 10001 100-01 2021-10-15 00860002273006 DoublecheQ Pregnancy Test Cassette 100-13 2019-06-03 B512200011 One Step Ovulation Test 20001 200-01 2021-10-15 B512210011 One Step Menopausal Test 21001 210-01 2021-10-15
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